A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834687



Internal ID22609622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141765692..141767491hg38UCSC Ensembl
chr3:141484534..141486333hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834687
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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